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T Cell Subset and Stimulation Strength-Dependent Modulation of T Cell Activation by Kv1.3 Blockers

Kv1.3 is a voltage-gated potassium channel expressed on T cells that plays an important role in T cell activation. Previous studies have shown that blocking Kv1.3 channels in human T cells during activation results in reduced calcium entry, cytokine production, and proliferation. The aim of the pres...

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Autores principales: Fung-Leung, Wai-Ping, Edwards, Wilson, Liu, Yi, Ngo, Karen, Angsana, Julianty, Castro, Glenda, Wu, Nancy, Liu, Xuejun, Swanson, Ronald V., Wickenden, Alan D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5249144/
https://www.ncbi.nlm.nih.gov/pubmed/28107393
http://dx.doi.org/10.1371/journal.pone.0170102
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author Fung-Leung, Wai-Ping
Edwards, Wilson
Liu, Yi
Ngo, Karen
Angsana, Julianty
Castro, Glenda
Wu, Nancy
Liu, Xuejun
Swanson, Ronald V.
Wickenden, Alan D.
author_facet Fung-Leung, Wai-Ping
Edwards, Wilson
Liu, Yi
Ngo, Karen
Angsana, Julianty
Castro, Glenda
Wu, Nancy
Liu, Xuejun
Swanson, Ronald V.
Wickenden, Alan D.
author_sort Fung-Leung, Wai-Ping
collection PubMed
description Kv1.3 is a voltage-gated potassium channel expressed on T cells that plays an important role in T cell activation. Previous studies have shown that blocking Kv1.3 channels in human T cells during activation results in reduced calcium entry, cytokine production, and proliferation. The aim of the present study was to further explore the effects of Kv1.3 blockers on the response of different human T cell subsets under various stimulation conditions. Our studies show that, unlike the immune suppressor cyclosporine A, the inhibitory effect of Kv1.3 blockers was partial and stimulation strength dependent, with reduced inhibitory efficacy on T cells under strengthened anti-CD3/CD28 stimulations. T cell responses to allergens including house dust mites and ragweed were partially reduced by Kv1.3 blockers. The effect of Kv1.3 inhibition was dependent on T cell subsets, with stronger effects on CCR7(-) effector memory compared to CCR7(+) central memory CD4 T cells. Calcium entry studies also revealed a population of CD4 T cells resistant to Kv1.3 blockade. Activation of CD4 T cells was accompanied with an increase in Kv1.3 currents but Kv1.3 transcripts were found to be reduced, suggesting a posttranscriptional mechanism in the regulation of Kv1.3 activities. In summary, Kv1.3 blockers inhibit T cell activation in a manner that is highly dependent on the T cell identity and stimulation strength, These findings suggest that Kv1.3 blockers inhibit T cells in a unique, conditional manner, further refining our understanding of the therapeutic potential of Kv1.3 blockers.
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spelling pubmed-52491442017-02-06 T Cell Subset and Stimulation Strength-Dependent Modulation of T Cell Activation by Kv1.3 Blockers Fung-Leung, Wai-Ping Edwards, Wilson Liu, Yi Ngo, Karen Angsana, Julianty Castro, Glenda Wu, Nancy Liu, Xuejun Swanson, Ronald V. Wickenden, Alan D. PLoS One Research Article Kv1.3 is a voltage-gated potassium channel expressed on T cells that plays an important role in T cell activation. Previous studies have shown that blocking Kv1.3 channels in human T cells during activation results in reduced calcium entry, cytokine production, and proliferation. The aim of the present study was to further explore the effects of Kv1.3 blockers on the response of different human T cell subsets under various stimulation conditions. Our studies show that, unlike the immune suppressor cyclosporine A, the inhibitory effect of Kv1.3 blockers was partial and stimulation strength dependent, with reduced inhibitory efficacy on T cells under strengthened anti-CD3/CD28 stimulations. T cell responses to allergens including house dust mites and ragweed were partially reduced by Kv1.3 blockers. The effect of Kv1.3 inhibition was dependent on T cell subsets, with stronger effects on CCR7(-) effector memory compared to CCR7(+) central memory CD4 T cells. Calcium entry studies also revealed a population of CD4 T cells resistant to Kv1.3 blockade. Activation of CD4 T cells was accompanied with an increase in Kv1.3 currents but Kv1.3 transcripts were found to be reduced, suggesting a posttranscriptional mechanism in the regulation of Kv1.3 activities. In summary, Kv1.3 blockers inhibit T cell activation in a manner that is highly dependent on the T cell identity and stimulation strength, These findings suggest that Kv1.3 blockers inhibit T cells in a unique, conditional manner, further refining our understanding of the therapeutic potential of Kv1.3 blockers. Public Library of Science 2017-01-20 /pmc/articles/PMC5249144/ /pubmed/28107393 http://dx.doi.org/10.1371/journal.pone.0170102 Text en © 2017 Fung-Leung et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Fung-Leung, Wai-Ping
Edwards, Wilson
Liu, Yi
Ngo, Karen
Angsana, Julianty
Castro, Glenda
Wu, Nancy
Liu, Xuejun
Swanson, Ronald V.
Wickenden, Alan D.
T Cell Subset and Stimulation Strength-Dependent Modulation of T Cell Activation by Kv1.3 Blockers
title T Cell Subset and Stimulation Strength-Dependent Modulation of T Cell Activation by Kv1.3 Blockers
title_full T Cell Subset and Stimulation Strength-Dependent Modulation of T Cell Activation by Kv1.3 Blockers
title_fullStr T Cell Subset and Stimulation Strength-Dependent Modulation of T Cell Activation by Kv1.3 Blockers
title_full_unstemmed T Cell Subset and Stimulation Strength-Dependent Modulation of T Cell Activation by Kv1.3 Blockers
title_short T Cell Subset and Stimulation Strength-Dependent Modulation of T Cell Activation by Kv1.3 Blockers
title_sort t cell subset and stimulation strength-dependent modulation of t cell activation by kv1.3 blockers
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5249144/
https://www.ncbi.nlm.nih.gov/pubmed/28107393
http://dx.doi.org/10.1371/journal.pone.0170102
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